Agapurin Sr 600

Leaflet accompanying the packaging: information for the user

Warning! The leaflet should be kept. Information on the immediate packaging in a foreign language.

AGAPURIN SR 600 (Pentoxifylline SR Zentiva 600 mg)

600 mg, prolonged-release tablets
Pentoxifylline
AGAPURIN SR 600 and Pentoxifylline SR Zentiva 600 mg are different trade names for the same medicine.

You should carefully read the contents of the leaflet before taking the medicine, as it contains important information for the patient.

• You should keep this leaflet, so that you can read it again if you need to.
• If you have any doubts, you should consult a doctor or pharmacist.
• This medicine has been prescribed specifically for you. Do not pass it on to others. The medicine may harm another person, even if their symptoms are the same as yours.
• If the patient experiences any side effects, including any side effects not listed in this leaflet, they should inform their doctor, pharmacist, or nurse. See section 4.

Table of contents of the leaflet:

• 1. What is Agapurin SR 600 and what is it used for
• 2. Important information before taking Agapurin SR 600
• 3. How to take Agapurin SR 600
• 4. Possible side effects
• 5. How to store Agapurin SR 600
• 6. Contents of the packaging and other information

1. What is Agapurin SR 600 and what is it used for

Indications for use of Agapurin SR 600:

• peripheral arterial and arteriovenous circulatory disorders caused by atherosclerosis, diabetes, as well as disorders of inflammatory or functional origin; intermittent claudication or rest pain, diabetic angiopathy, atherosclerotic disease of the arteries, trophic changes (post-thrombotic syndrome, leg ulcers, gangrene), angioneuropathies;
• circulatory disorders in the eye (acute and chronic circulatory disorders in the retina and choroid);
• disorders of the inner ear (hearing disorders, sudden hearing loss, etc.) caused by circulatory disorders;
• states of cerebral ischemia (post-stroke conditions, disorders of brain function of vascular origin with symptoms such as lack of concentration, dizziness, memory disorders, etc.).

Agapurin SR 600 is intended for use in adult patients.

2. Important information before taking Agapurin SR 600

When not to take Agapurin SR 600

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Warnings and precautions

Before starting treatment with Agapurin SR 600, you should discuss it with your doctor or pharmacist.
The doctor should consider the benefit-risk ratio of using Agapurin SR 600 in patients with arterial hypotension, severe heart rhythm disorders, advanced coronary and cerebral atherosclerosis, recent myocardial infarction, diabetes, severe renal function disorders.
If symptoms of anaphylactic or pseudo-anaphylactic reactions occur, you should discontinue use of Agapurin SR 600 and immediately contact your doctor.
During treatment with Agapurin SR 600, patients with severe heart rhythm disorders, advanced coronary and cerebral atherosclerosis with arterial hypotension and post-myocardial infarction should be under constant medical supervision.
Renal function disorders (creatinine clearance <30 ml min) and severe liver function disorders may cause delayed elimination of pentoxifylline. in such cases, the dose medicine should be reduced patient under constant medical supervision.
Patients with an increased tendency to bleeding, taking Agapurin SR 600 simultaneously with vitamin K antagonists, platelet aggregation inhibitors, or antidiabetic drugs should be under constant medical supervision.
Patients taking Agapurin SR 600 simultaneously with antidiabetic drugs should be under constant medical supervision (see "Agapurin SR 600 and other medicines", below).
Patients taking Agapurin SR 600 simultaneously with ciprofloxacin should be under constant medical supervision (see "Agapurin SR 600 and other medicines", below).
Patients taking pentoxifylline simultaneously with theophylline should be under constant medical supervision (see "Agapurin SR 600 and other medicines").

Agapurin SR 600 and other medicines

You should tell your doctor about all medicines you are currently taking or have recently taken, as well as any medicines you plan to take.
Agapurin SR 600 may enhance the effect of antihypertensive medicines (including angiotensin-converting enzyme inhibitors) or other medicines that lower blood pressure (e.g., nitrates).
In patients treated with insulin or oral antidiabetic medicines, after taking Agapurin SR 600, a decrease in blood glucose levels may occur. Therefore, diabetic patients should be under constant medical supervision.
In patients taking pentoxifylline simultaneously with vitamin K antagonists, cases of increased anticoagulant effect have been reported. When starting or modifying the dose of Agapurin SR 600 in these patients, close monitoring of anticoagulant activity is recommended.
Due to the increased risk of bleeding, caution should be exercised in patients taking pentoxifylline simultaneously with platelet aggregation inhibitors, such as clopidogrel, eptifibatide, tirofiban, epoprostenol, iloprost, abciximab, anagrelide, non-steroidal anti-inflammatory drugs other than selective COX-2 inhibitors, acetylsalicylic acid (aspirin) or lizine acetylsalicylate, ticlopidine, dipyridamole.
In some patients, concomitant use of pentoxifylline and theophylline may increase theophylline levels in the blood and enhance the adverse effects associated with its use.
In some patients, concomitant use of pentoxifylline and ciprofloxacin may increase pentoxifylline levels in the serum. Therefore, an increase in the frequency and severity of adverse effects associated with concomitant use of these two active substances may occur.
Concomitant use of Agapurin SR 600 with cimetidine may increase pentoxifylline and its active metabolite levels in the blood.

Agapurin SR 600 with food and drink

See section 3.

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a child, you should consult your doctor before taking this medicine.
This medicine is not recommended for use in pregnant or breastfeeding women.
In breastfeeding women, the doctor will decide whether the potential benefits outweigh the risks to the child.

Driving and using machines

This medicine has no influence on the ability to drive and use machines.

3. How to take Agapurin SR 600

This medicine should always be taken exactly as prescribed by your doctor. If you are unsure, consult your doctor or pharmacist.
The usual dose is one tablet once or twice a day.
Patients with low or variable blood pressure may require a special dosing schedule.
Dosing in patients with renal function disorders
In patients with renal function disorders (creatinine clearance <30 ml min), the doctor will reduce dose to 50-70% of usual recommended dose, depending on individual tolerance treatment.
Dosing in patients with liver function disorders
In patients with severe liver failure, the dose should be reduced. The decision on the dose used is made by the doctor, depending on the degree of liver failure and individual tolerance to treatment.
Use in children and adolescents
There is no experience with the use of this medicine in children.
Method of administration
Tablets should be swallowed whole during or immediately after a meal, with a sufficient amount of water.

Taking a higher dose of Agapurin SR 600 than recommended

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If you have taken more than the recommended dose of the medicine, you should immediately consult a doctor or pharmacist.
Initial symptoms may include nausea, dizziness, rapid heartbeat, hypotension, followed by fever, agitation, hot flashes, loss of consciousness, disappearance of reflexes, convulsions, and hematemesis (vomiting blood associated with gastrointestinal bleeding). Treatment of overdose is symptomatic. The patient may require intensive medical care in a hospital.
In case of overdose or accidental ingestion of the medicine by a child, you should immediately contact a doctor.

Missing a dose of Agapurin SR 600

If you have missed a dose of the medicine, you should take it as soon as possible. If it is almost time for the next dose, you should take only that dose at the scheduled time. Do not take a double dose to make up for the missed dose.

Stopping treatment with Agapurin SR 600

Without consulting a doctor, you should not stop taking the medicine.
If you have any further doubts about the use of this medicine, you should consult a doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.
You should immediately consult a doctor if you experience:

• symptoms of anaphylactic shock, disorientation, and fainting (due to circulatory disorders and a drop in blood pressure) or anaphylactic reactions, such as hives (urticaria), swelling of the face, eyelids, lips, mouth, or difficulty breathing. These conditions can be life-threatening.
• retinal hemorrhage.

You should immediately consult a doctor if you experience a tendency to bruise and bleed, as these may be symptoms of thrombocytopenia (reduced platelet count). In such cases, during treatment with Agapurin SR 600, the patient's blood morphology should be regularly monitored.
Gastrointestinal side effects are dose-dependent and usually disappear after discontinuation of treatment.
Side effects may occur with the following frequency:
Common (occurring in 1 to 10 patients out of 100): nausea, vomiting, bloating, abdominal pain, diarrhea.
Uncommon (occurring in 1 to 10 patients out of 1000): dizziness, headache, blurred vision, hot flashes.
Rare (occurring in 1 to 10 patients out of 10,000): allergic skin reactions, flushing (redness of the skin), itching, urticaria, increased sweating, cholestasis (bile stasis), increased liver enzyme activity (aminotransferases), hypotension (low blood pressure), tachycardia (rapid heart rate), palpitations (feeling of heartbeat), arrhythmias, angina pectoris (chest pain), anxiety, sleep disorders, hallucinations, hypoglycemia (low blood sugar levels), anaphylactic shock.
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Very rare (occurring in less than 1 in 10,000 patients): aplastic anemia, thrombocytopenia, bleeding (e.g., into the skin, mucous membranes, stomach, intestines).
Unknown (frequency cannot be estimated from available data): anaphylactic reaction, pseudo-anaphylactic reaction, leukopenia or neutropenia, agitation, angioedema (swelling of various body parts, most often in the face), rash, aseptic meningitis, gastrointestinal disorders, discomfort in the upper abdomen, feeling of fullness in the stomach (feeling of satiety), constipation, excessive salivation, decreased blood pressure, bronchospasm.

Reporting side effects

If you experience any side effects, including any side effects not listed in this leaflet, you should inform your doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Drug Safety, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Aleje Jerozolimskie 181C
02-222 Warsaw
phone: +48 22 49 21 301
fax: +48 22 49 21 309
website: https://smz.ezdrowie.gov.pl
By reporting side effects, you can help gather more information on the safety of this medicine.

5. How to store Agapurin SR 600

Store in a place out of sight and reach of children.
There are no special precautions for storage.
Do not use after the expiration date stated on the packaging. The expiration date is the last day of the specified month.
Medicines should not be disposed of via wastewater or household waste. You should ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.

6. Contents of the packaging and other information

What Agapurin SR 600 contains

The active substance of the medicine is pentoxifylline in the amount of 600 mg.
Other ingredients are: hypromellose 2208/15000, povidone 30, talc, magnesium stearate; coating:
Sepifilm 752 white (hypromellose, microcrystalline cellulose, polyoxyl 40 stearate, titanium dioxide (E 171)), simethicone emulsion SE4, macrogol 6000.

What Agapurin SR 600 looks like and what the packaging contains

White or almost white, oval, biconvex tablets with a dividing line on one side.
Pack size: 20, 50, or 100 prolonged-release tablets in blisters in a cardboard box.
For more detailed information, you should contact the marketing authorization holder or parallel importer.
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Marketing authorization holder in Romania, the country of export:

Zentiva a.s.
Einsteinova 24
85101 Bratislava
Slovak Republic

Manufacturer:

Saneca Pharmaceuticals a.s.
Nitrianska 100
92027 Hlohovec
Slovak Republic
Zentiva, k.s.
U kabelovny 130, Dolní Měcholupy
102 37, Prague 10
Czech Republic

Parallel importer:

Delfarma Sp. z o.o.
ul. Św. Teresy od Dzieciątka Jezus 111
91-222 Łódź

Repackaged by:

Delfarma Sp. z o.o.
ul. Św. Teresy od Dzieciątka Jezus 111
91-222 Łódź
Romanian marketing authorization number, country of export: 9192/2016/01
9192/2016/02
9192/2016/03

Parallel import authorization number: 578/12 Date of approval of the leaflet: 05.10.2022

[Information about the trademark]
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